A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186499



Internal ID20753539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:8915952..8936220hg38UCSC Ensembl
chr9:8915952..8936220hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3820269
hg1920269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6434014
Supporting Variants
Samples
Known GenesPTPRD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186499
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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